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HARVARD Citation
Eisfeldt, J. et al. (2022). Multi‐omics analysis reveals multiple mechanisms causing Prader–Willi like syndrome in a family with a X;15 translocation. Human mutation. 43 (11), pp. 1567-1575. [Online].
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Eisfeldt, J. et al. (2022). Multi‐omics analysis reveals multiple mechanisms causing Prader–Willi like syndrome in a family with a X;15 translocation. Human mutation. 43 (11), pp. 1567-1575. [Online].